Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:69640972-69641217 | Rare:52 | ||||
chr11:69675309-69675519 | Rare:56 | ||||
chr11:70398288-70398591 | Common:4; Rare:106 | ||||
chr11:71448367-71448681 | Common:3; Rare:79; Clinvar (benign):1 | ||||
chr11:72080444-72080853 | Common:2; Rare:91; Clinvar:7 | ||||
chr11:73597986-73598294 | Common:3; Rare:79 | ||||
chr11:73761053-73761408 | Common:3; Rare:91 | ||||
chr11:73876799-73877019 | Common:4; Rare:55 | ||||
chr11:74170865-74171341 | Common:2; Rare:150 | ||||
chr11:74949131-74949288 | Common:3; Rare:36 | ||||
chr11:76381112-76381348 | Common:3; Rare:74 | ||||
chr11:77637663-77637868 | Common:1; Rare:75 | ||||
chr11:78079813-78079939 | Common:2; Rare:43 | ||||
chr11:78139584-78139808 | Common:3; Rare:88; Clinvar:2 | ||||
chr11:83071827-83072111 | Common:4; Rare:80 |